HNF1A, HNF1 homeobox A, 6927

N. diseases: 292; N. variants: 105
Disease: Autoimmune Lymphoproliferative Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1328840
Disease: Autoimmune Lymphoproliferative Syndrome
Autoimmune Lymphoproliferative Syndrome 		0.010 Biomarker disease BEFREE With these examinations, we revealed that TCF1 deficiency relieved most manifestations of ALPS-like phenotype, which were caused by Fas mutation in TCF1<sup>-/-</sup> lpr/lpr mice. 28349581 2017